19 beste Stellen als site reliability in basel, bs – aktuell auf Personalsuche

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(Senior) Site Reliability Engineer (all genders)
adesso Schweiz —Basel, BS
Du bist ein erfahrener Site Reliability Engineer (SRE), der dafür sorgt, dass sowohl kundenbezogene Projekte als auch unsere internen Systemumgebungen…

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site reliability jobs near basel, bs

Member of the Quality Assurance Team at the GMP Facility for Advanced Therapies (80-90%)

Universität Basel -
Basel, BS

Jetzt bewerben

Details zur Stelle

Pensum: 90-100%
vor 1 Tag

Qualifikationen

Englisch
Bachelor
Produktion
Kommunikationsfähigkeit
Deutsch

Vollständige Stellenbeschreibung

As a joint venture of the University of Basel and the University Hospitals Basel, the Department of Biomedicine (DBM) brings together basic and clinical scientists to advance the understanding of health and disease.
We are home to more than 67 research groups and over 800 employees across six locations in the heart of Basel. Our collaborative and international environment fosters innovation, excellence, and impactful research.
The Core Facilities GMP led by Anke Wixmerten, is looking for a Member of the Quality Assurance Team (80-90%).
Join our community and help shape the future of biomedicine.

Your position

The state-of-the-art facilities on the USB campus provide all DBM researchers with access to a fully GMP-compliant environment for ATMP manufacturing and regulatory support for translational research projects and clinical trials. The GMP Facility for Advanced Therapies comprises two production sites and a core team of five people. A new facility together with the ETH Zürich is located at the Department of Biosystems Science and Engineering (DBSSE).

Responsibilities include

Assisting the transfer of processes from the DBM to the facility at the DBSSE
Supplier qualification and audits of material suppliers and service providers as well as material management
Assisting the core facility team and users with GMP-compliant documentation
Assisting users with the implementation of their projects (from research to GMP)
Participating in inspections by regulatory authorities and other audits
Validation of Quality Control Assays (FACS)

Your profile

The successful candidate should meet the following requirements

Experience in the GMP-compliant manufacturing of (preferably) ATMPs in a cleanroom facility (GMP) according to PIC/S and Swiss legislation
Excellent command of English (spoken and written), German is an asset
University degree in natural sciences (preferably biology)
Regulatory experience in a GMP environment
High level of reliability and a strong sense of responsibility
Excellent interpersonal and communication skills
Self-motivated and able to work both independently and as part of a team

We offer you

Opportunities to contribute to a wide range of projects focused on translating innovative ATMPs into clinical trials
Engaging work in a dynamic and international research environment
Attractive working conditions and salary in line with the standards of the University of Basel

Application / Contact

Please submit your application, including your resume, a description of your relevant experience, and contact information for references.
The position is available immediately or by agreement. For informal inquiries, please contact Anke Wixmerten ([email protected]).

Apply

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Erweiterte Suche

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